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培养的肝细胞在预测外源化学物肝毒性中的潜在应用。

The potential use of cultured hepatocytes in predicting the hepatotoxicity of xenobiotics.

作者信息

Gómez-Lechón M J, Montoya A, López P, Donato T, Larrauri A, Castell J V

机构信息

Centro de Investigación, Hospital La Fe, Valencia, Spain.

出版信息

Xenobiotica. 1988 Jun;18(6):725-35. doi: 10.3109/00498258809041711.

Abstract
  1. A protocol is proposed for screening for hepatotoxicity of xenobiotics in vitro in which hepatocytes exposed to the compounds are evaluated for both cytotoxic and metabolic effects. Four established hepatotoxins have been studied. 2. alpha-Amanitin at 1.5 pg/mg cell protein inhibited RNA synthesis by 93% and reduced albumin synthesis to 56% of the control after 13 h treatment. 3. D-Galactosamine at 40 microM inhibited glycogen synthesis by 31%, glucuronidation of p-nitrophenol by 13% and albumin synthesis by 10%, and produced an increase in cytosolic enzyme leakage. 4. Thioacetamide decreased ureogenesis after 24 h of treatment at 230 microM (31% inhibition) and after 48 h at 2.3 microM (25% inhibition). 5. Ultrastructural alterations of hepatocytes were found after 48 h exposure to 1 mM acetaminophen and were preceded by extensive leakage of the enzymes GOT and LDH. Membrane damage was observed after 24 h exposure to 0.1 mM acetaminophen.
摘要
  1. 提出了一种体外筛选异生物素肝毒性的方案,其中对暴露于化合物的肝细胞的细胞毒性和代谢作用进行评估。已对四种已确定的肝毒素进行了研究。2. 1.5 pg/mg细胞蛋白的α-鹅膏菌素在处理13小时后抑制RNA合成93%,并使白蛋白合成降至对照的56%。3. 40 microM的D-半乳糖胺抑制糖原合成31%,对硝基苯酚葡萄糖醛酸化13%,白蛋白合成10%,并导致细胞溶质酶泄漏增加。4. 硫代乙酰胺在230 microM处理24小时后(抑制31%)和在2.3 microM处理48小时后(抑制25%)降低尿素生成。5. 在暴露于1 mM对乙酰氨基酚48小时后发现肝细胞超微结构改变,且在此之前谷草转氨酶(GOT)和乳酸脱氢酶(LDH)大量泄漏。在暴露于0.1 mM对乙酰氨基酚24小时后观察到膜损伤。

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